ClinVar

NM_201253.3(CRB1):c.2306G>A (p.Arg769His)

Gene:

CRB1:crumbs cell polarity complex component 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q31.3

Genomic location:

• Chr1: 197427631 (on Assembly GRCh38)
• Chr1: 197396761 (on Assembly GRCh37)

Preferred name:

NM_201253.3(CRB1):c.2306G>A (p.Arg769His)

HGVS:

• NC_000001.11:g.197427631G>A
• NG_008483.2:g.231170G>A
• NM_001193640.2:c.1970G>A
• NM_001257965.2:c.2099G>A
• NM_001257966.2:c.2128+5675G>A
• NM_201253.3:c.2306G>AMANE SELECT
• NP_001180569.1:p.Arg657His
• NP_001244894.1:p.Arg700His
• NP_957705.1:p.Arg769His
• NP_957705.1:p.Arg769His
• NC_000001.10:g.197396761G>A
• NM_001257965.2:c.2099G>A
• NM_201253.2:c.2306G>A
• NR_047563.2:n.2259G>A
• NR_047564.2:n.2467G>A
• P82279:p.Arg769His

This HGVS expression did not pass validation

Protein change:

R657H

Links:

UniProtKB: P82279#VAR_022958; dbSNP: rs62636287

NCBI 1000 Genomes Browser:

rs62636287

Molecular consequence:

• NM_001257966.2:c.2128+5675G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001193640.2:c.1970G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001257965.2:c.2099G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_201253.3:c.2306G>A - missense variant - [Sequence Ontology: SO:0001583]
• NR_047563.2:n.2259G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_047564.2:n.2467G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]